%0 Journal Article %A H. Jayaprakash, S. %A Satheesh Krishna, B. %A Santhi Sudha, S. %A Bakthavatchala Reddy, N. %A Sreelakshmi, P. %A Madhu Kumar Reddy, K. %A Suresh Reddy, C. %D 2015 %T Ionic Liquid–Promoted Phospha-Michael Reaction: Convenient Access to β-Nitrophosphonates %U https://tandf.figshare.com/articles/journal_contribution/Ionic_Liquid_8211_Promoted_Phospha_Michael_Reaction_Convenient_Access_to_946_Nitrophosphonates/1463387 %R 10.6084/m9.figshare.1463387.v4 %2 https://ndownloader.figshare.com/files/2148464 %K Nitrophosphonate %K presence %K workup %K simplicity %K diazabicyclo %K Convenient Access %K method %K ionic %K reusability %K nitrostyrene %K DBUH %K room temperature %K Phosphite %K DBU %K procedure %X

A convenient and mild procedure is developed for β-nitrophosphonates via phospha-Michael addition of phosphites to nitrostyrene at room temperature in the presence of 1,8-diazabicyclo-[5.4.0]undec-7-ene (DBU)–based ionic liquid [DBUH][OAc]. The operational simplicity, convenient workup, and reusability of the ionic liquid make this method attractive.

%I Taylor & Francis